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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733008Generated: October 31, 2026

2-[3-Chloro-4-(2-pyrazolin-1-yl)phenyl]propionic acid → 2-[3-Chloro-4-(pyrazol-1-yl)phenyl]propionic acid

https://huagongshe.com/reaction/1733008

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-[3-Chloro-4-(2-pyrazolin-1-yl)phenyl]propionic acidHCID 20303541—
CatalystHCID 178418406HCID 178418406—
SolventTolueneHCID 1140—
Product2-[3-Chloro-4-(pyrazol-1-yl)phenyl]propionic acidHCID 20303500—

Reaction Steps

252 mg (1 mmole) of 2-[3-chloro-4-(2-pyrazolin-1-yl)phenyl]propionic acid are heated to the boil for 8 hours with 250 mg of active manganese dioxide and 1 g molecular sieve 4 A*) in 10 ml of toluene. Filtration is effected, followed by extraction first with 1 N hydrochloric acid and then with 1 N sodium hydroxide. The aqueous alkaline extract is acidified and subsequently extracted with benzene; the resulting organic phase is dried to yield 2-[3-chloro-4-(pyrazol-1-yl)phenyl]propionic acid (m.p. 83° to 85° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04239901
Source datasetuspto-grants-1980_12
ORD IDord-15935e0d3b914ef0a50bb9bb4da9d9e5
Source noteuspto-grants-1980_12